Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs2814778 0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 11
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 11
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs2738783 0.763 0.160 20 63677259 intron variant T/G snv 0.85 11
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs4129267 0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs4845604 0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs61839660 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs6894249 0.776 0.160 5 132461855 non coding transcript exon variant A/G snv 0.45 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs34290285 0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 8